[go: up one dir, main page]

NI201800071A - ISOINDOL COMPOUNDS - Google Patents

ISOINDOL COMPOUNDS

Info

Publication number
NI201800071A
NI201800071A NI201800071A NI201800071A NI201800071A NI 201800071 A NI201800071 A NI 201800071A NI 201800071 A NI201800071 A NI 201800071A NI 201800071 A NI201800071 A NI 201800071A NI 201800071 A NI201800071 A NI 201800071A
Authority
NI
Nicaragua
Prior art keywords
isoindol
compounds
compound
ror
mediated
Prior art date
Application number
NI201800071A
Other languages
Spanish (es)
Inventor
Lever Sarah
Narjes Frank
Ingemar Olsson Roine
Von Berg Stefan
Original Assignee
Astrazeneca Ab
Priority date (The priority date is an assumption and is not a legal conclusion. Google has not performed a legal analysis and makes no representation as to the accuracy of the date listed.)
Filing date
Publication date
Application filed by Astrazeneca Ab filed Critical Astrazeneca Ab
Publication of NI201800071A publication Critical patent/NI201800071A/en

Links

Classifications

    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61KPREPARATIONS FOR MEDICAL, DENTAL OR TOILETRY PURPOSES
    • A61K31/00Medicinal preparations containing organic active ingredients
    • A61K31/33Heterocyclic compounds
    • A61K31/395Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins
    • A61K31/40Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil
    • A61K31/403Heterocyclic compounds having nitrogen as a ring hetero atom, e.g. guanethidine or rifamycins having five-membered rings with one nitrogen as the only ring hetero atom, e.g. sulpiride, succinimide, tolmetin, buflomedil condensed with carbocyclic rings, e.g. carbazole
    • A61K31/4035Isoindoles, e.g. phthalimide
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P1/00Drugs for disorders of the alimentary tract or the digestive system
    • A61P1/04Drugs for disorders of the alimentary tract or the digestive system for ulcers, gastritis or reflux esophagitis, e.g. antacids, inhibitors of acid secretion, mucosal protectants
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P1/00Drugs for disorders of the alimentary tract or the digestive system
    • A61P1/18Drugs for disorders of the alimentary tract or the digestive system for pancreatic disorders, e.g. pancreatic enzymes
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P11/00Drugs for disorders of the respiratory system
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P11/00Drugs for disorders of the respiratory system
    • A61P11/06Antiasthmatics
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P11/00Drugs for disorders of the respiratory system
    • A61P11/12Mucolytics
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P17/00Drugs for dermatological disorders
    • A61P17/06Antipsoriatics
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P19/00Drugs for skeletal disorders
    • A61P19/02Drugs for skeletal disorders for joint disorders, e.g. arthritis, arthrosis
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P25/00Drugs for disorders of the nervous system
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P31/00Antiinfectives, i.e. antibiotics, antiseptics, chemotherapeutics
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P37/00Drugs for immunological or allergic disorders
    • AHUMAN NECESSITIES
    • A61MEDICAL OR VETERINARY SCIENCE; HYGIENE
    • A61PSPECIFIC THERAPEUTIC ACTIVITY OF CHEMICAL COMPOUNDS OR MEDICINAL PREPARATIONS
    • A61P43/00Drugs for specific purposes, not provided for in groups A61P1/00-A61P41/00
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D209/00Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom
    • C07D209/02Heterocyclic compounds containing five-membered rings, condensed with other rings, with one nitrogen atom as the only ring hetero atom condensed with one carbocyclic ring
    • C07D209/44Iso-indoles; Hydrogenated iso-indoles
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D405/00Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom
    • C07D405/02Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings
    • C07D405/06Heterocyclic compounds containing both one or more hetero rings having oxygen atoms as the only ring hetero atoms, and one or more rings having nitrogen as the only ring hetero atom containing two hetero rings linked by a carbon chain containing only aliphatic carbon atoms
    • CCHEMISTRY; METALLURGY
    • C07ORGANIC CHEMISTRY
    • C07DHETEROCYCLIC COMPOUNDS
    • C07D407/00Heterocyclic compounds containing two or more hetero rings, at least one ring having oxygen atoms as the only ring hetero atoms, not provided for by group C07D405/00
    • C07D407/02Heterocyclic compounds containing two or more hetero rings, at least one ring having oxygen atoms as the only ring hetero atoms, not provided for by group C07D405/00 containing two hetero rings
    • C07D407/06Heterocyclic compounds containing two or more hetero rings, at least one ring having oxygen atoms as the only ring hetero atoms, not provided for by group C07D405/00 containing two hetero rings linked by a carbon chain containing only aliphatic carbon atoms

Landscapes

  • Health & Medical Sciences (AREA)
  • Chemical & Material Sciences (AREA)
  • Organic Chemistry (AREA)
  • Public Health (AREA)
  • Pharmacology & Pharmacy (AREA)
  • Veterinary Medicine (AREA)
  • General Health & Medical Sciences (AREA)
  • Medicinal Chemistry (AREA)
  • Animal Behavior & Ethology (AREA)
  • Life Sciences & Earth Sciences (AREA)
  • Nuclear Medicine, Radiotherapy & Molecular Imaging (AREA)
  • General Chemical & Material Sciences (AREA)
  • Chemical Kinetics & Catalysis (AREA)
  • Engineering & Computer Science (AREA)
  • Bioinformatics & Cheminformatics (AREA)
  • Pulmonology (AREA)
  • Epidemiology (AREA)
  • Dermatology (AREA)
  • Immunology (AREA)
  • Rheumatology (AREA)
  • Physical Education & Sports Medicine (AREA)
  • Orthopedic Medicine & Surgery (AREA)
  • Biomedical Technology (AREA)
  • Oncology (AREA)
  • Communicable Diseases (AREA)
  • Neurology (AREA)
  • Neurosurgery (AREA)
  • Pharmaceuticals Containing Other Organic And Inorganic Compounds (AREA)
  • Indole Compounds (AREA)
  • Plural Heterocyclic Compounds (AREA)
  • Medicines That Contain Protein Lipid Enzymes And Other Medicines (AREA)

Abstract

La presente memoria proporciona un compuesto de fórmula (I): (I) o una sal farmacéuticamente aceptable del mismo; un procedimiento para preparar un compuesto tal; y al uso de tal compuesto en el tratamiento de una ROR? y o estado de enfermedad / ROR?t mediada.The present specification provides a compound of formula (I): (I) or a pharmaceutically acceptable salt thereof; a process for preparing such a compound; and to the use of such a compound in the treatment of an ROR? and or disease state / ROR? t mediated.

NI201800071A 2015-12-15 2018-06-13 ISOINDOL COMPOUNDS NI201800071A (en)

Applications Claiming Priority (1)

Application Number Priority Date Filing Date Title
US201562267391P 2015-12-15 2015-12-15

Publications (1)

Publication Number Publication Date
NI201800071A true NI201800071A (en) 2018-10-18

Family

ID=57708552

Family Applications (1)

Application Number Title Priority Date Filing Date
NI201800071A NI201800071A (en) 2015-12-15 2018-06-13 ISOINDOL COMPOUNDS

Country Status (27)

Country Link
US (4) US10011566B2 (en)
EP (1) EP3390396B1 (en)
JP (1) JP6448867B2 (en)
KR (1) KR101947976B1 (en)
CN (1) CN109071516B (en)
AR (1) AR107054A1 (en)
AU (1) AU2016374294B2 (en)
BR (1) BR112018011851A2 (en)
CA (1) CA3007893A1 (en)
CL (1) CL2018001573A1 (en)
CO (1) CO2018005983A2 (en)
CR (1) CR20180328A (en)
DO (1) DOP2018000148A (en)
EA (1) EA034514B1 (en)
ES (1) ES2927631T3 (en)
IL (1) IL259818B (en)
MX (1) MX376029B (en)
MY (1) MY196276A (en)
NI (1) NI201800071A (en)
PE (1) PE20181319A1 (en)
PH (1) PH12018501237A1 (en)
SG (1) SG11201804587QA (en)
SV (1) SV2018005713A (en)
TN (1) TN2018000188A1 (en)
TW (1) TWI728017B (en)
WO (1) WO2017102784A1 (en)
ZA (1) ZA201804618B (en)

Families Citing this family (8)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
KR101947976B1 (en) 2015-12-15 2019-02-13 아스트라제네카 아베 Isoindole compound
EP3638661A1 (en) 2017-06-14 2020-04-22 Astrazeneca AB 2,3-dihydroisoindole-1-carboxamides useful as ror-gamma modulators
WO2020035557A1 (en) * 2018-08-17 2020-02-20 Leo Pharma A/S Novel heteroaromatic modulators of the retinoid-related orphan receptor gamma
WO2020035556A1 (en) * 2018-08-17 2020-02-20 Leo Pharma A/S Novel heteroaromatic modulators of the retinoid-related orphan receptor gamma
CN113666863B (en) * 2020-05-15 2024-06-11 励缔(杭州)医药科技有限公司 Biaryl compounds useful as rory modulators
CA3178650A1 (en) * 2020-05-15 2021-11-18 Yaobang CHENG Aniline compound used as ror.gamma. regulator
KR102422891B1 (en) 2022-01-26 2022-07-20 (주)셀시스템 Integrated solar hot water and battery charging device with AI-based priority control function and charging method using the same
WO2023232870A1 (en) 2022-05-31 2023-12-07 Immunic Ag Rorg/rorgt modulators for the treatment of virus infections like covid-19

Family Cites Families (74)

* Cited by examiner, † Cited by third party
Publication number Priority date Publication date Assignee Title
GB9414139D0 (en) 1994-07-13 1994-08-31 Smithkline Beecham Plc Novel compounds
EP0944387A1 (en) 1996-01-30 1999-09-29 Merck & Co., Inc. Inhibitors of farnesyl-protein transferase
SK12782000A3 (en) 1998-02-25 2001-04-09 Genetics Institute, Inc. Inhibitors of phospholipase a2
US6316503B1 (en) 1999-03-15 2001-11-13 Tularik Inc. LXR modulators
CA2377999A1 (en) 1999-07-08 2001-01-18 Tularik Inc Compositions and methods for raising hdl cholesterol levels
ATE310728T1 (en) 2000-05-11 2005-12-15 Bristol Myers Squibb Co TETRAHYDROISOCHINOLINE ANALOGUE AS GROWTH HORMONE SECRETAGOGEN
US6777446B2 (en) 2000-09-05 2004-08-17 Tularik, Inc. FXR modulators
EP1341765A1 (en) 2000-12-07 2003-09-10 AstraZeneca AB Therapeutic compounds
ES2284817T3 (en) 2001-01-26 2007-11-16 Chugai Seiyaku Kabushiki Kaisha PROCEDURES FOR THE TREATMENT OF DISEASES WITH INHIBITORS OF MALONIL COA DESCARBOXYLASE.
US6649606B1 (en) 2001-11-09 2003-11-18 Bristol-Myers Squibb Co. Tetrahydroisoquinoline analogs as modulators of chemokine receptor activity
JP2005533007A (en) 2002-03-27 2005-11-04 スミスクライン・ビーチャム・コーポレイション Treatment method using LXR modulator
AU2003227689A1 (en) 2002-04-29 2003-11-17 Novartis Ag Crystal structure of the ligand binding domain of the retinoic acid-related orphan receptor alpha (ror-alpha)
EP1646394A2 (en) 2003-07-22 2006-04-19 Glaxo Group Limited Methods of treatment with lxr agonists
WO2005013946A2 (en) 2003-07-28 2005-02-17 Glaxo Group Limited Methods of treatment inflammatory bowel with lxr agonists
WO2005055998A1 (en) 2003-12-04 2005-06-23 Smithkline Beecham Corporation Methods of treatment with lxr agonists
WO2006091862A2 (en) 2005-02-24 2006-08-31 Kemia, Inc. Cytokine inhibitors and their use in therapy
WO2007058990A2 (en) 2005-11-14 2007-05-24 Kemia, Inc. Therapy using cytokine inhibitors
WO2007055374A1 (en) 2005-11-14 2007-05-18 Mitsubishi Tanabe Pharma Corporation Therapeutic agent for osteoporosis
PE20071025A1 (en) 2006-01-31 2007-10-17 Mitsubishi Tanabe Pharma Corp TRISUSTITUTED AMINE COMPOUND
AR059826A1 (en) 2006-03-13 2008-04-30 Univ California UREA INHIBITORS CONFORMATIONALLY RESTRICTED OF SOLUBLE HYDROLASSE EPOXIDE
WO2007146712A2 (en) 2006-06-09 2007-12-21 Kemia, Inc. Therapy using cytokine inhibitors
TW200812962A (en) 2006-07-12 2008-03-16 Astrazeneca Ab New compounds I/418
CN101490002A (en) * 2006-07-12 2009-07-22 阿斯利康(瑞典)有限公司 3-oxoisoindoline-1-carboxamide derivatives as analgesic agents
CL2007002670A1 (en) 2006-09-15 2008-05-16 Celgene Corp Soc Organizada Ba COMPOUNDS DERIVED FROM N-METHYLAMINEOME-ISOINDOLINE; PHARMACEUTICAL COMPOSITION; DOSAGE FORM, USEFUL TO TREAT OR PREVENT DISEASES SUCH AS CANCER, PAIN, PULMONARY DISORDER, CNS DISORDER AND ATEROSCLEROSIS.
JP4834699B2 (en) 2007-07-30 2011-12-14 田辺三菱製薬株式会社 Pharmaceutical composition
JP4846769B2 (en) 2007-07-30 2011-12-28 田辺三菱製薬株式会社 Pharmaceutical composition
WO2011115892A1 (en) * 2010-03-15 2011-09-22 Griffin Patrick R Modulators of the retinoic acid receptor-related orphan receptors
WO2012027965A1 (en) 2010-09-01 2012-03-08 Glaxo Group Limited Novel compounds
WO2012028100A1 (en) 2010-09-01 2012-03-08 Glaxo Group Limited Novel compounds
WO2012100732A1 (en) 2011-01-24 2012-08-02 Glaxo Group Limited Retinoid-related orphan receptor gamma modulators, composition containing them and uses thereof
WO2012100734A1 (en) 2011-01-24 2012-08-02 Glaxo Group Limited Compounds useful as retinoid-related orphan receptor gamma modulators
EP2487159A1 (en) 2011-02-11 2012-08-15 MSD Oss B.V. RorgammaT inhibitors
WO2012158784A2 (en) 2011-05-16 2012-11-22 Theodore Mark Kamenecka Modulators of the nuclear hormone receptor ror
WO2013029338A1 (en) 2011-09-01 2013-03-07 Glaxo Group Limited Novel compounds
WO2013100027A1 (en) 2011-12-28 2013-07-04 武田薬品工業株式会社 Heterocyclic compound
US9365512B2 (en) 2012-02-13 2016-06-14 AbbVie Deutschland GmbH & Co. KG Isoindoline derivatives, pharmaceutical compositions containing them, and their use in therapy
US9321750B2 (en) 2012-04-20 2016-04-26 Innov17 Llc ROR modulators and their uses
EP2844260A4 (en) 2012-04-30 2016-06-29 Anderson Gaweco Ror modulators and their uses
EP2844259A4 (en) 2012-04-30 2015-11-11 Anderson Gaweco Ror modulators and their uses
KR101936851B1 (en) * 2012-07-16 2019-01-11 한국과학기술연구원 Pyrazolopyridine or indazole derivatives as protein kinase inhibitors
WO2013171729A2 (en) 2013-01-08 2013-11-21 Glenmark Pharmaceuticals S.A. Aryl and heteroaryl amide compounds as rorgamat modulator
WO2014125426A1 (en) 2013-02-15 2014-08-21 Aurigene Discovery Technologies Limited Trisubstituted heterocyclic derivatives as ror gamma modulators
WO2014165816A1 (en) 2013-04-05 2014-10-09 North Carolina Central University Compounds useful for the treatment of metabolic disorders and synthesis of the same
EP2991994B1 (en) 2013-05-01 2018-08-15 Vitae Pharmaceuticals, Inc. Thiazolopyrrolidine inhibitors of ror-gamma
WO2015002230A1 (en) 2013-07-03 2015-01-08 武田薬品工業株式会社 Amide compound
EP3018126A4 (en) 2013-07-03 2016-12-07 Takeda Pharmaceuticals Co HETEROCYCLIC COMPOUND
EP3027616B1 (en) 2013-07-30 2018-01-10 Boehringer Ingelheim International GmbH Azaindole compounds as modulators of rorc
US9745267B2 (en) 2013-09-05 2017-08-29 Boehringer Ingelheim International Gmbh Compounds as modulators of RORC
TN2016000224A1 (en) 2013-12-05 2017-10-06 Lead Pharma Holding Bv Ror gamma (rory) modulators
WO2015083130A1 (en) 2013-12-06 2015-06-11 Aurigene Discovery Technologies Limited Fused pyridine and pyrimidine derivatives as ror gamma modulators
WO2015101928A1 (en) 2013-12-31 2015-07-09 Aurigene Discovery Technologies Limited Fused thiophene and thiazole derivatives as ror gamma modulators
JP6466461B2 (en) 2014-02-03 2019-02-06 ヴァイティー ファーマシューティカルズ,インコーポレイテッド Dihydropyrrolopyridine inhibitors of ROR gamma
JPWO2015129853A1 (en) 2014-02-27 2017-03-30 東レ株式会社 Cyclic amine derivatives and their pharmaceutical use
US11084784B2 (en) 2014-03-27 2021-08-10 Piramal Enterprises Limited ROR-gamma modulators and uses thereof
BR112016021962A2 (en) 2014-04-14 2023-01-20 Boehringer Ingelheim Int COMPOUNDS, PHARMACEUTICAL COMPOSITION AND THEIR USES AS GAMMA ROR MODULATORS
SG11201607518RA (en) 2014-04-16 2016-10-28 Glenmark Pharmaceuticals Sa Aryl and heteroaryl ether compounds as ror gamma modulators
AU2015285142B2 (en) 2014-07-01 2019-02-21 Takeda Pharmaceutical Company Limited Heterocyclic compounds and their use as Retinoid-related orphan receptor (ROR) gamma-T inhibitors
DK3177612T3 (en) 2014-08-04 2022-05-16 Nuevolution As POSSIBLE FUSIONED HETEROCYCLYL-SUBSTITUTED PYRIMIDINE DERIVATIVES USE FOR THE TREATMENT OF INFLAMMATORY, METABOLIC, ONCOLOGICAL AND AUTO-IMMUNE DISEASES
MA40759A (en) 2014-09-26 2017-08-01 Pfizer PYRROLOPYRIDINE-SUBSTITUTED BY METHYL AND TRIFLUOROMETHYL RORC2 MODULATORS AND THEIR METHODS OF USE
JP6564029B2 (en) 2014-10-14 2019-08-21 ヴァイティー ファーマシューティカルズ,エルエルシー Dihydropyrrolopyridine inhibitors of ROR-gamma
EP3215152A4 (en) 2014-11-05 2018-06-13 The University of Kansas SMALL MOLECULE INHIBITORS OF THE MITOCHONDRIAL PERMEABILITY TRANSITION PORE (mtPTP)
US9663515B2 (en) 2014-11-05 2017-05-30 Vitae Pharmaceuticals, Inc. Dihydropyrrolopyridine inhibitors of ROR-gamma
US9845308B2 (en) 2014-11-05 2017-12-19 Vitae Pharmaceuticals, Inc. Isoindoline inhibitors of ROR-gamma
US20180110774A1 (en) 2015-04-28 2018-04-26 Stc. Unm Compositions and methods for treatment of pulmonary hypertension
DK3294713T5 (en) 2015-05-15 2021-05-31 Aurigene Discovery Tech Ltd SUBSTITUTED TETRAHYDROQUINOLINONE COMPOUNDS AS TUBE-GAMMA MODULATORS
EP3101005A1 (en) 2015-06-05 2016-12-07 Lead Pharma Cel Models IP B.V. Ror gamma (rory) modulators
EP3101008A1 (en) 2015-06-05 2016-12-07 Lead Pharma Cel Models IP B.V. Ror gamma (rory) modulators
EP3101009A1 (en) 2015-06-05 2016-12-07 Lead Pharma Cel Models IP B.V. Ror gamma (rory) modulators
EP3101007A1 (en) 2015-06-05 2016-12-07 Lead Pharma Cel Models IP B.V. Ror gamma (rory) modulators
EP3101006A1 (en) 2015-06-05 2016-12-07 Lead Pharma Cel Models IP B.V. Ror gamma (rory) modulators
WO2017010399A1 (en) 2015-07-10 2017-01-19 塩野義製薬株式会社 COMPOUNDS HAVING RORγt INHIBITORY EFFECTS AND PHARMACEUTICAL COMPOSITIONS CONTAINING THE SAME
EP3331876B1 (en) 2015-08-05 2020-10-07 Vitae Pharmaceuticals, LLC Modulators of ror-gamma
JP6778259B2 (en) 2015-10-01 2020-10-28 ベーリンガー インゲルハイム インターナショナル ゲゼルシャフト ミット ベシュレンクテル ハフツング Pteridine derivative as a modulator of ROR gamma
KR101947976B1 (en) 2015-12-15 2019-02-13 아스트라제네카 아베 Isoindole compound

Also Published As

Publication number Publication date
CR20180328A (en) 2018-08-09
WO2017102784A9 (en) 2018-04-05
CO2018005983A2 (en) 2018-06-20
IL259818B (en) 2021-05-31
US11453644B1 (en) 2022-09-27
EA034514B1 (en) 2020-02-14
EP3390396A1 (en) 2018-10-24
SG11201804587QA (en) 2018-06-28
WO2017102784A1 (en) 2017-06-22
AU2016374294A1 (en) 2018-07-19
JP6448867B2 (en) 2019-01-09
CA3007893A1 (en) 2017-06-22
CL2018001573A1 (en) 2018-07-27
TW201738210A (en) 2017-11-01
US10011566B2 (en) 2018-07-03
CN109071516A (en) 2018-12-21
IL259818A (en) 2018-07-31
MX2018007296A (en) 2019-01-10
ES2927631T3 (en) 2022-11-08
US10526286B2 (en) 2020-01-07
MY196276A (en) 2023-03-24
US20170166527A1 (en) 2017-06-15
AU2016374294B2 (en) 2019-06-27
CN109071516B (en) 2021-08-31
DOP2018000148A (en) 2018-07-15
ZA201804618B (en) 2020-09-30
US20200181084A1 (en) 2020-06-11
AR107054A1 (en) 2018-03-14
SV2018005713A (en) 2018-08-08
US20190084934A1 (en) 2019-03-21
PH12018501237A1 (en) 2019-02-18
TWI728017B (en) 2021-05-21
KR20180086269A (en) 2018-07-30
KR101947976B1 (en) 2019-02-13
MX376029B (en) 2025-03-07
BR112018011851A2 (en) 2018-12-04
JP2018537485A (en) 2018-12-20
EP3390396B1 (en) 2022-07-06
US10988445B2 (en) 2021-04-27
PE20181319A1 (en) 2018-08-14
EA201891342A1 (en) 2019-01-31
TN2018000188A1 (en) 2019-10-04

Similar Documents

Publication Publication Date Title
NI201800071A (en) ISOINDOL COMPOUNDS
DOP2019000168A (en) AMINO-TRIAZOLOPIRIDINE COMPOUNDS AND THEIR USE IN CANCER TREATMENT
CO2017004525A2 (en) Ror-gamma inhibitory dihydropyrrolopyridines
CO2017002998A2 (en) Tetrahydronaphthalene derivatives that inhibit mcl-1 protein
CL2017000379A1 (en) Pyrrolopyrimidine compounds used as toll receptor agonists. 7 (tlr7)
AR103680A1 (en) BACE1 SELECTIVE INHIBITORS
CO2018004857A2 (en) Dihydroimidazopirazinone derivatives used in cancer treatment
CL2016001918A1 (en) Heteroaryl amides as protein aggregation inhibitors
GT201500053A (en) PHARMACEUTICAL COMPOSITION COVERED WITH REGORAFENIB
MX2016015434A (en) Pharmaceutical combinations for treating cancer.
ECSP16084317A (en) PHARMACEUTICAL FORMULATIONS, PREPARATION PROCESSES AND METHODS OF USE
MX2020003732A (en) FUSIONED RING DERIVATIVE AS AN A2A RECEPTOR INHIBITOR.
MX377172B (en) COMBINATION FORMULA OF TESOFENSINE AND BETA-BLOCKER
CL2017000682A1 (en) Novel imidazopyridazine compounds and their use.
CR20160527A (en) CARBOXAMIDE DERIVATIVES
MX390977B (en) Methods for improving myocardial performance in patients with Fontan surgery using udenafil compounds
CO2019007186A2 (en) Ror gamma modulators (rorγ)
CL2016001843A1 (en) Use of a composition comprising a) a compound of defined formula (ia) or a salt thereof and b) a pharmaceutically acceptable carrier or excipient to prepare a medicament useful for treating an allergic condition in a mammal.
SV2018005701A (en) 1,3,4-TIADIAZOL COMPOUNDS AND THEIR USE IN CANCER TREATMENT
UY36084A (en) POLICYCLIC HERG ACTIVATORS
AR113817A1 (en) COMPOUNDS USEFUL TO INHIBIT CDK7
UY35743A (en) SYNTHESIS PROCEDURE FOR THE PREPARATION OF C1-CETO MACROCICLIC ANALOGS OF HALICONDRINE B AND USEFUL INTERMEDIARIES IN THE SAME